Variant report

Variant	nsv894683
Chromosome Location	chr9:140913833-141153431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2558)
CpG islands
(count:2017)
Chromatin interactive
region (count:62)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2558 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:141020689-141020889	GM12878	blood:	n/a	n/a
2	ATF3	chr9:141020692-141020855	GM12878	blood:	n/a	n/a
3	ATF3	chr9:141020637-141020864	K562	blood:	n/a	n/a
4	ATF3	chr9:141054176-141054450	A549	lung:	n/a	n/a
5	BACH1	chr9:140918133-140918313	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr9:141082701-141083207	GM12878	blood:	n/a	chr9:141082765-141082773
7	BATF	chr9:141121222-141121626	GM12878	blood:	n/a	n/a
8	BATF	chr9:141107515-141107806	GM12878	blood:	n/a	n/a
9	BATF	chr9:141020609-141020912	GM12878	blood:	n/a	n/a
10	BATF	chr9:141128400-141128680	GM12878	blood:	n/a	n/a
11	BATF	chr9:141118240-141118564	GM12878	blood:	n/a	chr9:141118380-141118391
12	BATF	chr9:141128455-141128723	GM12878	blood:	n/a	n/a
13	BATF	chr9:141064102-141064298	GM12878	blood:	n/a	n/a
14	BATF	chr9:141054182-141054368	GM12878	blood:	n/a	n/a
15	BATF	chr9:141118278-141118550	GM12878	blood:	n/a	chr9:141118380-141118391
16	BATF	chr9:141113007-141113243	GM12878	blood:	n/a	n/a
17	BATF	chr9:141107608-141107779	GM12878	blood:	n/a	n/a
18	BATF	chr9:141114113-141114462	GM12878	blood:	n/a	n/a
19	BATF	chr9:141121304-141121639	GM12878	blood:	n/a	n/a
20	BATF	chr9:141112985-141113342	GM12878	blood:	n/a	n/a
21	BATF	chr9:141115173-141115405	GM12878	blood:	n/a	n/a
22	BATF	chr9:141023409-141023594	GM12878	blood:	n/a	n/a
23	BATF	chr9:141050185-141050584	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:141118215-141118496	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:141023414-141023612	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:141126990-141127300	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:141122785-141122963	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:141121270-141121610	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:141128328-141128725	GM12878	blood:	n/a	n/a
30	BCL11A	chr9:141114024-141114388	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:141115303-141115593	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:141129767-141129926	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:141114056-141114418	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:141115227-141115417	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:141117472-141117648	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:141128443-141128816	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:141054194-141054361	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:141067698-141067987	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:141054141-141054402	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:141121234-141121658	GM12878	blood:	n/a	n/a
41	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:141061417-141061666	HepG2	liver:	n/a	n/a
43	BHLHE40	chr9:141044398-141044667	HepG2	liver:	n/a	n/a
44	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
45	BHLHE40	chr9:141121159-141121509	HepG2	liver:	n/a	n/a
46	BHLHE40	chr9:141118206-141118545	HepG2	liver:	n/a	n/a
47	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
48	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
49	BHLHE40	chr9:140993888-140994157	HepG2	liver:	n/a	n/a
50	CBX3	chr9:140980114-140980383	K562	blood:	n/a	n/a

(count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:141012312-141012362	HCF	heart:	n/a
2	chr9:141105974-141106024	GM12892	blood:	n/a
3	chr9:140957018-140957068	SAEC	small airway:	n/a
4	chr9:141105974-141106024	MCF10A-Er-Src	breast:	n/a
5	chr9:141012312-141012362	HCF	heart:	n/a
6	chr9:141105974-141106024	GM12892	blood:	n/a
7	chr9:140957018-140957068	SAEC	small airway:	n/a
8	chr9:141105974-141106024	MCF10A-Er-Src	breast:	n/a
9	chr9:140917413-140917463	HRCEpiC	kidney:	n/a
10	chr9:141013537-141013587	AG04450	lung:	fetal
11	chr9:141022253-141022303	MCF-7	breast:	n/a
12	chr9:140917413-140917463	NHBE	bronchial:	n/a
13	chr9:141016791-141016841	U87	brain:	n/a
14	chr9:141016791-141016841	PANC-1	pancreas:	n/a
15	chr9:140939374-140939424	HIPEpiC	eye:	n/a
16	chr9:141042453-141042503	HEEpiC	esophagus:	n/a
17	chr9:141105974-141106024	Hepatocyte	liver:	n/a
18	chr9:140916980-140917030	MCF10A-Er-Src	breast:	n/a
19	chr9:141069847-141069897	H1-hESC	embryonic stem cell:	embryo
20	chr9:141016791-141016841	SK-N-SH_RA	brain:	n/a
21	chr9:141013112-141013162	Caco-2	colon:	n/a
22	chr9:141105974-141106024	HCPEpiC	choroid plexus:	n/a
23	chr9:141042435-141042485	HCM	heart:	n/a
24	chr9:141111396-141111446	ovcar-3	ovarian:	n/a
25	chr9:141105974-141106024	GM19239	blood:	n/a
26	chr9:140916078-140916128	RPTEC	kidney:	n/a
27	chr9:140917413-140917463	RPTEC	kidney:	n/a
28	chr9:141017001-141017051	HIPEpiC	eye:	n/a
29	chr9:141007633-141007683	SKMC	muscle:	n/a
30	chr9:141105202-141105252	SK-N-SH	brain:	n/a
31	chr9:140970188-140970238	HepG2	liver:	n/a
32	chr9:141013537-141013587	K562	blood:	n/a
33	chr9:140939374-140939424	SK-N-MC	brain:	n/a
34	chr9:140939374-140939424	AG10803	skin:	n/a
35	chr9:140939579-140939629	HepG2	liver:	n/a
36	chr9:141111396-141111446	RPTEC	kidney:	n/a
37	chr9:141014674-141014724	HRCEpiC	kidney:	n/a
38	chr9:140917431-140917481	ProgFib	skin:	n/a
39	chr9:141111396-141111446	AG04449	skin:	fetal
40	chr9:140939374-140939424	PANC-1	pancreas:	n/a
41	chr9:140937920-140937970	ProgFib	skin:	n/a
42	chr9:141012312-141012362	HCM	heart:	n/a
43	chr9:140917431-140917481	CMK	blood:	n/a
44	chr9:141045017-141045067	BE2_C	brain:	n/a
45	chr9:141017001-141017051	AG09309	skin:	n/a
46	chr9:141067944-141067994	PFSK-1	brain:	n/a
47	chr9:141105974-141106024	AG09319	gingival:	n/a
48	chr9:141017001-141017051	HRPEpiC	eye:	n/a
49	chr9:141111396-141111446	SK-N-SH	brain:	n/a
50	chr9:140937920-140937970	SAEC	small airway:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
2	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
3	chr1:811815..813428-chr9:141073371..141075327,2	K562	blood:
4	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
5	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
6	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
7	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
8	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
9	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
10	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
11	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
12	chr9:140958325..140960613-chr9:140962095..140963626,2	K562	blood:
13	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
14	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
15	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
16	chr9:140962197..140963909-chr9:140964440..140967429,2	K562	blood:
17	chr9:140769881..140772281-chr9:140919838..140921575,2	K562	blood:
18	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
19	chr10:122219..122922-chr9:141042181..141042681,2	MCF-7	breast:
20	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
21	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
22	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
23	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
24	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
25	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
26	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
27	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
28	chr9:140867124..140870002-chr9:140953480..140955243,2	MCF-7	breast:
29	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
30	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
31	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
32	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
33	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
34	chr10:122225..122779-chr9:141041705..141042205,2	MCF-7	breast:
35	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
36	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
37	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:
38	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
39	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
40	chr9:140969366..140972281-chr9:140974102..140976549,3	MCF-7	breast:
41	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
42	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
43	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
44	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
45	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
46	chr9:137024514..137025058-chr9:141013083..141013583,2	HCT-116	colon:
47	chr9:140966280..140969244-chr9:140971233..140973098,3	K562	blood:
48	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
49	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
50	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-7	chr9:140954809-140955130	NONHSAT135765
2	lnc-AL772363.1-7	chr9:140954806-140956852	NONHSAT135764
3	lnc-CACNA1B-1	chr9:141141988-141142607	XLOC_007621
4	lnc-AL772363.1-6	chr9:140939331-140939523	NONHSAT135763
5	lnc-AL772363.1-6	chr9:140934955-140937453	NONHSAT135763
6	lnc-AL772363.1-7	chr9:140955477-140955599	NONHSAT135765
7	lnc-CACNA1B-1	chr9:141139721-141139830	XLOC_007621
8	lnc-AL772363.1-6	chr9:140937901-140938239	NONHSAT135763

No data

Variant related genes	Relation type
ENSG00000237419	TF binding region
RNU6-785P	TF binding region
TUBBP5	TF binding region
ENSG00000229926	TF binding region
FAM157B	TF binding region
CACNA1B	TF binding region
ENSG00000237419	CpG island
RNU6-785P	CpG island
TUBBP5	CpG island
ENSG00000229926	CpG island
FAM157B	CpG island
CACNA1B	CpG island
ENSG00000148408	chromatin interactions
ENSG00000230368	chromatin interactions

Extended variants
information (count: 7651 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:7651 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56323036	chr9:140913833-140913834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560294940	chr9:140913920-140913921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532603075	chr9:140913957-140913958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552725888	chr9:140913994-140913995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112695280	chr9:140913997-140913998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571430201	chr9:140914031-140914032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530707051	chr9:140914035-140914036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550528761	chr9:140914051-140914052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567546755	chr9:140914091-140914092	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs558028803	chr9:140914092-140914093	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs11137339	chr9:140914093-140914094	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs186567368	chr9:140914095-140914096	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140872371	chr9:140914096-140914097	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374227050	chr9:140914104-140914105	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs115509525	chr9:140914124-140914125	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs145410208	chr9:140914131-140914132	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs530964181	chr9:140914168-140914169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190897570	chr9:140914186-140914187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575030020	chr9:140914215-140914216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544378985	chr9:140914230-140914231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114561035	chr9:140914238-140914239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561185042	chr9:140914265-140914266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117984085	chr9:140914273-140914274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147668849	chr9:140914276-140914277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560509740	chr9:140914277-140914278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532566233	chr9:140914288-140914289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148716893	chr9:140914304-140914305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562947050	chr9:140914325-140914326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546821794	chr9:140914348-140914349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11137340	chr9:140914383-140914384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532566203	chr9:140914401-140914402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11137341	chr9:140914448-140914449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183663933	chr9:140914456-140914457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529955189	chr9:140914497-140914498	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs75939392	chr9:140914548-140914549	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572600255	chr9:140914551-140914552	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs4066675	chr9:140914570-140914571	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546603651	chr9:140914642-140914643	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs566096675	chr9:140914652-140914653	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs112623068	chr9:140914673-140914674	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs551784468	chr9:140914685-140914686	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs151006249	chr9:140914701-140914702	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs537552820	chr9:140914764-140914765	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs555097328	chr9:140914771-140914772	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs574955548	chr9:140914829-140914830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367713326	chr9:140914875-140914876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534472497	chr9:140914881-140914882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140845472	chr9:140914957-140914958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150146368	chr9:140914970-140914971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538343452	chr9:140914993-140914994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:19)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD

Chromatin state (count:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140894600-140916600	Weak transcription	Brain Anterior Caudate	brain
2	chr9:140902400-140917000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:140902600-140916800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr9:140902800-140917600	Weak transcription	Right Atrium	heart
5	chr9:140903800-140917000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr9:140904600-140917000	Weak transcription	Spleen	Spleen
7	chr9:140904800-140917000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:140905000-140915600	Weak transcription	Brain Angular Gyrus	brain
9	chr9:140905200-140917000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr9:140908800-140916200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:140910800-140916400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:140912200-140914600	Weak transcription	Fetal Brain Female	brain
13	chr9:140912200-140914800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr9:140912200-140915400	Weak transcription	Brain Germinal Matrix	brain
15	chr9:140912400-140916200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr9:140915000-140915200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr9:140915200-140915400	Bivalent Enhancer	Fetal Brain Female	brain
18	chr9:140915200-140915600	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
19	chr9:140916200-140917000	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr9:140916200-140917600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr9:140916200-140917600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr9:140916200-140918600	Enhancers	Pancreas	Pancrea
23	chr9:140916400-140916800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:140916600-140916800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
25	chr9:140916600-140916800	Bivalent Enhancer	Brain Angular Gyrus	brain
26	chr9:140916600-140917000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
27	chr9:140916600-140917000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr9:140916600-140917000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr9:140916600-140917000	Bivalent Enhancer	Brain Anterior Caudate	brain
30	chr9:140916600-140917200	Bivalent Enhancer	Brain Hippocampus Middle	brain
31	chr9:140916600-140917400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
32	chr9:140916600-140917400	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr9:140916600-140917400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
34	chr9:140916600-140917600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
35	chr9:140916800-140917000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr9:140916800-140917000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
37	chr9:140916800-140917000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr9:140916800-140917000	Bivalent Enhancer	Brain Germinal Matrix	brain
39	chr9:140916800-140917200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
40	chr9:140916800-140917200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
41	chr9:140916800-140917200	Bivalent Enhancer	Fetal Brain Female	brain
42	chr9:140916800-140917400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
43	chr9:140916800-140917600	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr9:140916800-140917800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:140916800-140917800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr9:140917000-140917200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
47	chr9:140917000-140917200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
48	chr9:140917000-140917200	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr9:140917000-140917200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:140917000-140917200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood

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